1. Identifying regulatory and procedural challenges
2. Providing budgetary and timeframe guidelines
3. Consulting on India and site selection  
4. Assessment of  the likelihood of performing a particular study in India

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5. Protocol ethical standards and challenges
6. Verification of possible recruitment rates and determining the number of sites required for a completion of a study within a designated time period
7. Feasibility of local purchase of concomitant and study drugs and other clinical materials
8. Vendor identification and comparison for services inclduign, but not limited to, blinding, packaging, IVRS, maintenance of eCRF infrastructure, laboratories, remote reading of ECGs.

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9. Other services as desired by sponsor

Key to our strength in conducting such feasibility studies is a comprehensive updated data of medical organizations listed in India which includes comprehensive data on investigators; most of them are personally known to us and have worked with them. Proscizen has access to such opinion leaders across therapeutic areas in the country.